DOI: 10.1055/s-00000041

Neuropediatrics

Ausgabe 02 · Volume 16 · Mai 1985 DOI: 10.1055/s-002-10749

ORIGINAL ARTICLES

  • 59
    Meencke, H. J.; Gerhard, C.:

    Morphological Aspects of Aetiology and the Course of Infantile Spasms (West-Syndrome)1

  • 67
    Wolburg-Buchholz, Karen; Schlote, W.; Baumkötter, J.; Cantz, M.; Holder, H.; Harzer, K.:

    Familial Lysosomal Storage Disease with Generalized Vacuolization and Sialic Aciduria. Sporadic Salla Disease

  • 76
    Takashima, S.; Mito, T.; Becker, L. E.:

    Neuronal Development in the Medullary Reticular Formation in Sudden Infant Death Syndrome and Premature Infants

  • 80
    Baier, W. K.; Doose, H.:

    Petit Mal-Absences of Childhood Onset: Familial Prevalences of Migraine and Seizures*

  • 84
    Baier, W. K.:

    Genetics of Migraine and Migraine Accompagneé: A Study of Eighty-One Children and Their Families*

  • 92
    Behbehani, A. W.:

    Termination of Strict Diet Therapy in Phenylketonuria*

    A Study on EEG Sleep Patterns and Computer Spectral Analysis
  • 106
    Simmonds, H. A.; Webster, D. R.; Lingam, S.; Wilson, J.:

    An Inborn Error of Purine Metabolism, Deafness and Neurodevelopmental Abnormality

  • 109
    Yamano, T.; Shimada, M.; Sugino, H.; Dezawa, T.; Koike, M.; Okada, S.; Yabuuchi, H.:

    Ultrastructural Study on a Severe Infantile Sialidosis (β-Galactosidase - α-Neuraminidase Deficiency)

    • CASE REPORTS

  • 98
    Wisniewski, K.; Rudelli, R.; Laure-Kamionowska, M.; Sklower, S.; Houck, G. E.; Kieras Jr, F.; Ramos, P.; Wisniewski, H. M.; Braak, H.:

    Sanfilippo Disease, Type A with some Features of Ceroid Lipofuscinosis